4gy0

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{{STRUCTURE_4gy0| PDB=4gy0 | SCENE= }}
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==Round 18 Arylesterase Variant of Phosphotriesterase==
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===Round 18 Arylesterase Variant of Phosphotriesterase===
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<StructureSection load='4gy0' size='340' side='right' caption='[[4gy0]], [[Resolution|resolution]] 1.85&Aring;' scene=''>
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{{ABSTRACT_PUBMED_23212386}}
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4gy0]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4GY0 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4GY0 FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4e3t|4e3t]], [[4gy1|4gy1]]</td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Aryldialkylphosphatase Aryldialkylphosphatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.8.1 3.1.8.1] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4gy0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4gy0 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4gy0 RCSB], [http://www.ebi.ac.uk/pdbsum/4gy0 PDBsum]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Optimization processes, such as evolution, are constrained by diminishing returns-the closer the optimum, the smaller the benefit per mutation, and by tradeoffs-improvement of one property at the cost of others. However, the magnitude and molecular basis of these parameters, and their effect on evolutionary transitions, remain unknown. Here we pursue a complete functional transition of an enzyme with a &gt;10(9)-fold change in the enzyme's selectivity using laboratory evolution. We observed strong diminishing returns, with the initial mutations conferring &gt;25-fold higher improvements than later ones, and asymmetric tradeoffs whereby the gain/loss ratio of the new/old activity decreased 400-fold from the beginning of the trajectory to its end. We describe the molecular basis for these phenomena and suggest they have an important role in shaping natural proteins. These findings also suggest that the catalytic efficiency and specificity of many natural enzymes may be far from their optimum.
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==About this Structure==
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Diminishing returns and tradeoffs constrain the laboratory optimization of an enzyme.,Tokuriki N, Jackson CJ, Afriat-Jurnou L, Wyganowski KT, Tang R, Tawfik DS Nat Commun. 2012 Dec 4;3:1257. doi: 10.1038/ncomms2246. PMID:23212386<ref>PMID:23212386</ref>
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[[4gy0]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4GY0 OCA].
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==Reference==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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<ref group="xtra">PMID:023212386</ref><references group="xtra"/><references/>
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</div>
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==See Also==
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*[[Phosphotriesterase|Phosphotriesterase]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
[[Category: Aryldialkylphosphatase]]
[[Category: Aryldialkylphosphatase]]
[[Category: Synthetic construct]]
[[Category: Synthetic construct]]
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[[Category: Jackson, C J.]]
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[[Category: Jackson, C J]]
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[[Category: Tawfik, D S.]]
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[[Category: Tawfik, D S]]
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[[Category: Tokuriki, N.]]
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[[Category: Tokuriki, N]]
[[Category: Alpha/beta hydrolase]]
[[Category: Alpha/beta hydrolase]]
[[Category: Arylesterase]]
[[Category: Arylesterase]]
[[Category: Hydrolase]]
[[Category: Hydrolase]]

Revision as of 10:56, 21 December 2014

Round 18 Arylesterase Variant of Phosphotriesterase

4gy0, resolution 1.85Å

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